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FDA 510(k)

PILLING DISPOSABLE AORTA PUNCH

K-Number: K854915 · 1986-01-24

ApplicantPilling Co.
Decision Date1986-01-24
Product Code
DecisionSubstantially Equivalent

Device Summary

PILLING DISPOSABLE AORTA PUNCH is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1986-01-24 under 510(k) number K854915. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PILLING DISPOSABLE AORTA PUNCH?

PILLING DISPOSABLE AORTA PUNCH is a medical device that received FDA 510(k) clearance on 1986-01-24. The listed applicant is Pilling Co.. The 510(k) number is K854915.

When did PILLING DISPOSABLE AORTA PUNCH receive FDA 510(k) clearance?

PILLING DISPOSABLE AORTA PUNCH received FDA 510(k) clearance on 1986-01-24, under 510(k) number K854915.

Who is the listed applicant for PILLING DISPOSABLE AORTA PUNCH?

The FDA 510(k) record lists Pilling Co. as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Pilling Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K934427PILLING LAPAROSCOPIC INSTRUMENTATIONK925370TRIANGULAR JAW MICROLARYNGEAL FORCEPSK925198KAISER NO CANNULA THORACOSCOPY/LAPAROSCOPY INSTRK922971NO-SCALPEL VASCETOMY INSTRUMENTSK914015CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMPK911099MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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